Karen Posted October 30, 2006 Share Posted October 30, 2006 I would be interested to know if anybody else has had a third nerve palsy due to their SAH. My eye was totally shut after the SAH and even though it's opened up, my vision on the right side is still slightly slower. I'm now 15 months post SAH and I've found that it has affected me probably worse than the actual SAH. Now undergoing physio for my brain to adapt to being outside of its comfort zone.......I still have some double vision and pain when I look up, especially to the left. It's affected many aspects of my life and still makes me feel dizzy and unbalanced. I have found it pretty debilitating, but I'm sure that I can't be the only one out there to have had this. Look forward to hearing from you. Karen x Quote Link to comment Share on other sites More sharing options...
Join the conversation
You can post now and register later. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.